Variant report

Variant	esv3503622
Chromosome Location	chr6:57916040-58522258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1672)
CpG islands
(count:2628)
Chromatin interactive
region (count:3)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1672 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:57996881-57996935	K562	blood:	n/a	n/a
2	ATF2	chr6:58312840-58313086	GM12878	blood:	n/a	n/a
3	ATF2	chr6:58287667-58287899	GM12878	blood:	n/a	n/a
4	ATF2	chr6:58226933-58227385	GM12878	blood:	n/a	n/a
5	ATF2	chr6:58287566-58287962	GM12878	blood:	n/a	n/a
6	ATF2	chr6:58226948-58227297	GM12878	blood:	n/a	n/a
7	ATF2	chr6:58225246-58225574	GM12878	blood:	n/a	n/a
8	ATF3	chr6:58142478-58142721	A549	lung:	n/a	n/a
9	ATF3	chr6:58142472-58142715	K562	blood:	n/a	n/a
10	ATF3	chr6:58149095-58149601	K562	blood:	n/a	n/a
11	ATF3	chr6:58141691-58142004	K562	blood:	n/a	n/a
12	BATF	chr6:58312874-58313176	GM12878	blood:	n/a	chr6:58313100-58313108
13	BATF	chr6:58274740-58275182	GM12878	blood:	n/a	chr6:58274977-58274988
14	BATF	chr6:58274807-58275130	GM12878	blood:	n/a	chr6:58274977-58274988
15	BATF	chr6:58312874-58313181	GM12878	blood:	n/a	chr6:58313100-58313108
16	BATF	chr6:58241654-58241917	GM12878	blood:	n/a	chr6:58241758-58241769
17	BATF	chr6:58225176-58225639	GM12878	blood:	n/a	n/a
18	BATF	chr6:58192220-58192422	GM12878	blood:	n/a	n/a
19	BATF	chr6:58226989-58227547	GM12878	blood:	n/a	n/a
20	BATF	chr6:58226995-58227530	GM12878	blood:	n/a	n/a
21	BATF	chr6:58326544-58326859	GM12878	blood:	n/a	n/a
22	BATF	chr6:58241206-58241440	GM12878	blood:	n/a	chr6:58241313-58241322 chr6:58241337-58241348
23	BATF	chr6:58159860-58160064	GM12878	blood:	n/a	n/a
24	BATF	chr6:58241686-58241892	GM12878	blood:	n/a	chr6:58241758-58241769
25	BATF	chr6:58225149-58225723	GM12878	blood:	n/a	n/a
26	BATF	chr6:58205099-58205316	GM12878	blood:	n/a	n/a
27	BATF	chr6:58287533-58287892	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:58312858-58313167	GM12878	blood:	n/a	chr6:58313103-58313112
29	BCL11A	chr6:58245996-58246178	GM12878	blood:	n/a	n/a
30	BCL11A	chr6:58225136-58225637	GM12878	blood:	n/a	n/a
31	BCL11A	chr6:58287319-58287843	GM12878	blood:	n/a	n/a
32	BCL11A	chr6:58227066-58227268	GM12878	blood:	n/a	n/a
33	BCL11A	chr6:58312939-58313153	GM12878	blood:	n/a	chr6:58313103-58313112
34	BCL11A	chr6:58205087-58205300	GM12878	blood:	n/a	n/a
35	BCL11A	chr6:58287570-58287800	GM12878	blood:	n/a	n/a
36	BCL11A	chr6:58226962-58227383	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:58312816-58313161	GM12878	blood:	n/a	chr6:58313103-58313112
38	BCLAF1	chr6:58287452-58288025	GM12878	blood:	n/a	n/a
39	BCLAF1	chr6:58287548-58287910	GM12878	blood:	n/a	n/a
40	BHLHE40	chr6:58312965-58313069	GM12878	blood:	n/a	n/a
41	CBX3	chr6:58287493-58287955	K562	blood:	n/a	n/a
42	CBX3	chr6:58287498-58287998	K562	blood:	n/a	n/a
43	CCNT2	chr6:58287622-58287859	K562	blood:	n/a	n/a
44	CEBPB	chr6:58146782-58147007	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:58287720-58287958	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr6:58167948-58168069	A549	lung:	n/a	chr6:58168013-58168026 chr6:58168014-58168025
47	CEBPB	chr6:58357831-58357857	HepG2	liver:	n/a	chr6:58357833-58357844 chr6:58357834-58357845
48	CEBPB	chr6:58262027-58262420	K562	blood:	n/a	n/a
49	CEBPB	chr6:58030489-58030521	HepG2	liver:	n/a	chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499 chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499
50	CEBPB	chr6:58167907-58168057	K562	blood:	n/a	chr6:58168013-58168026 chr6:58168014-58168025

(count:2628 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:58399599-58399649	HCPEpiC	choroid plexus:	n/a
2	chr6:58180750-58180800	HEEpiC	esophagus:	n/a
3	chr6:58263193-58263243	BJ	skin:	n/a
4	chr6:58399793-58399843	SK-N-MC	brain:	n/a
5	chr6:58287827-58287877	Hela-S3	cervix:	n/a
6	chr6:58399599-58399649	HCPEpiC	choroid plexus:	n/a
7	chr6:58180750-58180800	HEEpiC	esophagus:	n/a
8	chr6:58263193-58263243	BJ	skin:	n/a
9	chr6:58399793-58399843	SK-N-MC	brain:	n/a
10	chr6:58287827-58287877	Hela-S3	cervix:	n/a
11	chr6:58180750-58180800	GM19239	blood:	n/a
12	chr6:57972721-57972771	BJ	skin:	n/a
13	chr6:58141890-58141940	U87	brain:	n/a
14	chr6:58147897-58147947	U87	brain:	n/a
15	chr6:58148485-58148535	HRE	kidney:	n/a
16	chr6:58172067-58172117	AG04449	skin:	fetal
17	chr6:58001971-58002021	NH-A	brain:	n/a
18	chr6:58287825-58287875	SK-N-MC	brain:	n/a
19	chr6:57972680-57972730	HIPEpiC	eye:	n/a
20	chr6:58148810-58148860	Hepatocyte	liver:	n/a
21	chr6:58148898-58148948	SK-N-MC	brain:	n/a
22	chr6:58148485-58148535	NT2-D1	testis:	n/a
23	chr6:58141890-58141940	GM19239	blood:	n/a
24	chr6:58287827-58287877	SK-N-SH	brain:	n/a
25	chr6:58182993-58183043	HAEpiC	amniotic membrane:	n/a
26	chr6:58141890-58141940	RPTEC	kidney:	n/a
27	chr6:57972721-57972771	SK-N-SH	brain:	n/a
28	chr6:58142044-58142094	HEEpiC	esophagus:	n/a
29	chr6:57972349-57972399	AoSMC	blood vessel:	n/a
30	chr6:58289118-58289168	MCF10A-Er-Src	breast:	n/a
31	chr6:57970666-57970716	CMK	blood:	n/a
32	chr6:58289131-58289181	HepG2	liver:	n/a
33	chr6:57970592-57970642	NB4	blood:	n/a
34	chr6:58147897-58147947	SK-N-MC	brain:	n/a
35	chr6:58286735-58286785	GM12891	blood:	n/a
36	chr6:57972721-57972771	ProgFib	skin:	n/a
37	chr6:58289118-58289168	BE2_C	brain:	n/a
38	chr6:58399599-58399649	Hela-S3	cervix:	n/a
39	chr6:58148485-58148535	HEK293	kidney:	embryo
40	chr6:57972721-57972771	HNPCEpiC	eye:	n/a
41	chr6:58287430-58287480	AG10803	skin:	n/a
42	chr6:58182993-58183043	HRPEpiC	eye:	n/a
43	chr6:58147625-58147675	NT2-D1	testis:	n/a
44	chr6:58147897-58147947	SK-N-SH	brain:	n/a
45	chr6:58172356-58172406	HEK293	kidney:	embryo
46	chr6:58148554-58148604	HRCEpiC	kidney:	n/a
47	chr6:58148898-58148948	T-47D	breast:	n/a
48	chr6:58172356-58172406	U87	brain:	n/a
49	chr6:58263193-58263243	NT2-D1	testis:	n/a
50	chr6:58180096-58180146	ECC-1	luminal epithelium:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:58293670..58295896-chr6:58296442..58300027,3	K562	blood:
2	chr6:58293670..58295896-chr6:58296442..58298545,2	K562	blood:
3	chr5:37379216..37379885-chr6:58287233..58287739,2	Hela-S3	cervix:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB23-3	chr6:58275087-58275346	NONHSAT113319
2	lnc-RAB23-3	chr6:58234838-58240189	ENSG00000272316.1
3	lnc-RAB23-3	chr6:58275196-58275346	NONHSAT113311
4	lnc-RAB23-18	chr6:58228887-58229426	ENSG00000271761.1
5	lnc-RAB23-3	chr6:58285306-58285389	NONHSAT113319
6	lnc-RAB23-3	chr6:58272400-58273455	NONHSAT113318
7	lnc-RAB23-16	chr6:58182169-58182746	ENSG00000272541.1
8	lnc-RAB23-3	chr6:58287430-58287502	NONHSAT113319
9	lnc-RAB23-3	chr6:58287599-58287654	NONHSAT113317
10	lnc-BAG2-12	chr6:58290606-58290988	l_3195_chr6:58290605-58295048_testes
11	lnc-RAB23-3	chr6:58287430-58287502	NONHSAT113317
12	lnc-RAB23-17	chr6:58186881-58187205	NONHSAT113305
13	lnc-BAG2-6	chr6:58291908-58292021	ENSG00000225096
14	lnc-RAB23-3	chr6:58275196-58275417	NONHSAT113318
15	lnc-BAG2-7	chr6:58488888-58489027	ENSG00000223633.2
16	lnc-BAG2-6	chr6:58297873-58297934	ENSG00000225096
17	lnc-RAB23-3	chr6:58287599-58287654	NONHSAT113319
18	lnc-BAG2-6	chr6:58298372-58298496	ENSG00000225096
19	lnc-RAB23-4	chr6:58275151-58276677	ENSG00000215190
20	lnc-RAB23-4	chr6:58272361-58273455	ENSG00000215190
21	lnc-BAG2-4	chr6:58186873-58187271	XLOC_005332
22	lnc-RAB23-3	chr6:58272350-58273455	NONHSAT113311
23	lnc-BAG2-5	chr6:58243460-58243544	ENSG00000236143.1
24	lnc-BAG2-12	chr6:58294832-58295048	l_3195_chr6:58290605-58295048_testes
25	lnc-BAG2-7	chr6:58513504-58513860	ENSG00000223633.2
26	lnc-RAB23-3	chr6:58239194-58239687	XLOC_005753
27	lnc-BAG2-7	chr6:58488888-58489027	ENSG00000223633.1
28	lnc-BAG2-5	chr6:58243374-58243434	ENSG00000236143.1
29	lnc-RAB23-19	chr6:58397998-58399412	NONHSAT113321
30	lnc-RAB23-3	chr6:58272393-58273455	NONHSAT113317
31	lnc-RAB23-17	chr6:58192326-58192620	NONHSAT113305
32	lnc-RAB23-3	chr6:58275196-58275346	NONHSAT113310
33	lnc-BAG2-4	chr6:58182220-58183029	XLOC_005332
34	lnc-RAB23-3	chr6:58276137-58276366	NONHSAT113310
35	lnc-RAB23-3	chr6:58272350-58273455	NONHSAT113310
36	lnc-RAB23-3	chr6:58285306-58285389	NONHSAT113317
37	lnc-RAB23-3	chr6:58275636-58276125	NONHSAT113311
38	lnc-RAB23-3	chr6:58234692-58238642	XLOC_005753

No data

Variant related genes	Relation type
ENSG00000272316	TF binding region
ENSG00000272541	TF binding region
ENSG00000270213	TF binding region
LINC00680	TF binding region
GAPDHP15	TF binding region
ENSG00000271761	TF binding region
ENSG00000225096	TF binding region
GUSBP4	TF binding region
ENSG00000223633	TF binding region
POM121L14P	TF binding region
ENSG00000216687	TF binding region
RBBP4P4	TF binding region
ENSG00000272316	CpG island
ENSG00000272541	CpG island
ENSG00000270213	CpG island
LINC00680	CpG island
GAPDHP15	CpG island
ENSG00000271761	CpG island
ENSG00000225096	CpG island
GUSBP4	CpG island
ENSG00000223633	CpG island
POM121L14P	CpG island
ENSG00000216687	CpG island
RBBP4P4	CpG island
ENSG00000082068	chromatin interactions
ENSG00000214563	chromatin interactions

Extended variants
information (count: 5169 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:5169 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150589529	chr6:57916064-57916065	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs373022655	chr6:57916115-57916116	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs571358855	chr6:57916120-57916121	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs372632996	chr6:57916183-57916184	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs545075746	chr6:57916207-57916208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140292301	chr6:57916225-57916226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142719973	chr6:57916320-57916321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7758590	chr6:57916338-57916339	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs561191176	chr6:57916366-57916367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531613360	chr6:57916380-57916381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549746201	chr6:57916399-57916400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs3125349	chr6:57916407-57916408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147373711	chr6:57916412-57916413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567053160	chr6:57916420-57916421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532544772	chr6:57916464-57916465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547489097	chr6:57916483-57916484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565796921	chr6:57916484-57916485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374715141	chr6:57916621-57916622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4395724	chr6:57916630-57916631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4403257	chr6:57916650-57916651	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs548148746	chr6:57916661-57916662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570279768	chr6:57916767-57916768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537733545	chr6:57916802-57916803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555696760	chr6:57916840-57916841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs5005209	chr6:57916841-57916842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535176705	chr6:57916856-57916857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185003780	chr6:57916861-57916862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572145149	chr6:57916872-57916873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189514478	chr6:57916894-57916895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554536270	chr6:57916917-57916918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575828907	chr6:57916943-57916944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115245544	chr6:57916951-57916952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182155893	chr6:57916971-57916972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116035055	chr6:57917009-57917010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9476375	chr6:57917024-57917025	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs528557113	chr6:57917082-57917083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540795137	chr6:57917095-57917096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372437668	chr6:57917096-57917097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374355637	chr6:57917114-57917115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559441163	chr6:57917139-57917140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530110987	chr6:57917145-57917146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548211082	chr6:57917152-57917153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570023479	chr6:57917154-57917155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531153257	chr6:57917174-57917175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539486528	chr6:57917219-57917220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185857492	chr6:57917229-57917230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs397839778	chr6:57917240-57917241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188755357	chr6:57917248-57917249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535245088	chr6:57917253-57917254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs397839779	chr6:57917258-57917259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1189 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57915400-57916200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr6:57915400-57916200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:57915400-57916200	Active TSS	NHEK	skin
4	chr6:57916200-57917600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:57916200-57917600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:57916200-57917600	Weak transcription	NHEK	skin
7	chr6:57916800-57917800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr6:57917200-57918200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:57917200-57919000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr6:57917400-57918400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr6:57917400-57918600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr6:57917400-57919800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr6:57917600-57918200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr6:57917600-57918200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:57917600-57918200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:57917600-57918200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:57917600-57918200	Enhancers	NHEK	skin
18	chr6:57917800-57919600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr6:57918000-57918600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:57918000-57918600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr6:57918200-57919000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr6:57918200-57919200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:57918200-57919600	Weak transcription	NHEK	skin
24	chr6:57919000-57919400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr6:57919000-57919800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr6:57919200-57919400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:57919400-57919800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr6:57919600-57919800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr6:57919600-57921600	Enhancers	NHEK	skin
30	chr6:57920000-57920400	Enhancers	HMEC	breast
31	chr6:57944400-57944800	Enhancers	Fetal Brain Male	brain
32	chr6:58141200-58141600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr6:58141400-58141800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
34	chr6:58141400-58143200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
35	chr6:58141400-58143400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
36	chr6:58141600-58141800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr6:58141600-58141800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr6:58141600-58141800	Bivalent Enhancer	Brain Germinal Matrix	brain
39	chr6:58141600-58141800	Bivalent Enhancer	Placenta	Placenta
40	chr6:58141600-58141800	Bivalent Enhancer	NHDF-Ad	bronchial
41	chr6:58141600-58142000	Bivalent Enhancer	HUVEC	blood vessel
42	chr6:58141600-58142000	Active TSS	K562	blood
43	chr6:58141600-58142200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
44	chr6:58141600-58142200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr6:58141600-58142200	Bivalent Enhancer	Fetal Muscle Leg	muscle
46	chr6:58141600-58142400	Active TSS	H1 Cell Line	embryonic stem cell
47	chr6:58141600-58143000	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr6:58141600-58143000	Active TSS	H9 Cell Line	embryonic stem cell
49	chr6:58141600-58143000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
50	chr6:58141600-58143000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell

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